Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
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DOID:10652 | Alzheimer's disease | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:10652 | Alzheimer's disease | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:3144 | cutis laxa | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:3627 | aortic aneurysm | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:3827 | congenital diaphragmatic hernia | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:12377 | spinal muscular atrophy | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:0111196 | X-linked distal spinal muscular atrophy 3 | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:890 | mitochondrial encephalomyopathy | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:11758 | iron deficiency anemia | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:12377 | spinal muscular atrophy | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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DOID:3827 | congenital diaphragmatic hernia | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:893 | Wilson disease | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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DOID:0050866 | oral squamous cell carcinoma | MGI:1913585 | Mus musculus (house mouse) | 66335 | Atp6v1c1 |
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DOID:5517 | stomach carcinoma | MGI:1913585 | Mus musculus (house mouse) | 66335 | Atp6v1c1 |
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DOID:0080720 | autosomal dominant congenital deafness with onychodystrophy | MGI:109618 | Mus musculus (house mouse) | 11966 | Atp6v1b2 |
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DOID:14219 | renal tubular acidosis | MGI:109618 | Mus musculus (house mouse) | 11966 | Atp6v1b2 |
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DOID:1826 | epilepsy | MGI:109618 | Mus musculus (house mouse) | 11966 | Atp6v1b2 |
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DOID:0050873 | follicular lymphoma | MGI:109618 | Mus musculus (house mouse) | 11966 | Atp6v1b2 |
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DOID:0112275 | developmental and epileptic encephalopathy 93 | MGI:1201780 | Mus musculus (house mouse) | 11964 | Atp6v1a |
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DOID:0070129 | autosomal recessive cutis laxa type IID | MGI:1201780 | Mus musculus (house mouse) | 11964 | Atp6v1a |
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DOID:1432 | blindness | MGI:1328318 | Mus musculus (house mouse) | 11974 | Atp6v0e |
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DOID:0070134 | autosomal recessive cutis laxa type IIA | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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DOID:0112171 | wrinkly skin syndrome | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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DOID:14219 | renal tubular acidosis | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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DOID:0110942 | autosomal recessive osteopetrosis 1 | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024